Olivia Knight

Vater/vacterl Association, also known as vacterl association, is related to vacterl association, x-linked, with or without hydrocephalus and vacterl association with hydrocephalus. An important gene associated with Vater/vacterl Association is HOXD13 (Homeobox D13). The drugs Nicotinamide and Niacin have been mentioned in the context of this ...

Lymphoproliferative Syndrome, X-Linked, 1, also known as lymphomatoid papulosis, is related to primary cutaneous anaplastic large cell lymphoma and lymphoproliferative syndrome, x-linked, 2. An important gene associated with Lymphoproliferative Syndrome, X-Linked, 1 is SH2D1A (SH2 Domain Containing 1A), and among its related ...

Sezary's Disease, also known as sezary syndrome, is related to primary cutaneous t-cell non-hodgkin lymphoma and lymphoma, hodgkin, classic, and has symptoms including pruritus An important gene associated with Sezary's Disease is BCL10 (BCL10 Immune Signaling Adaptor), and among its related pathways/superpathways are Innate Immune System ...

Myotonic Disease, also known as myotonic disorders, is related to myotonic dystrophy 2 and hyperkalemic periodic paralysis, and has symptoms including muscle cramp, muscle rigidity and muscle spasticity. An important gene associated with Myotonic Disease is DMPK (DM1 Protein Kinase), and among its related pathways/superpathways is ...

Haim-Munk Syndrome, also known as keratosis palmoplantaris with periodontopathia and onychogryposis, is related to periodontitis and contractural arachnodactyly, congenital. An important gene associated with Haim-Munk Syndrome is CTSC (Cathepsin C). Affiliated tissues include skin and bone, and related phenotypes are pes planus and ...